Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Multiple System Atrophy and COQ2[original query] |
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| Mutations in COQ2 in familial and sporadic multiple-system atrophy. The New England journal of medicine 2013 Jul 369 (3): 233-44. Authors are not available |
| COQ2 p.V393A variant, rs148156462, is not associated with Parkinson's disease in a Taiwanese population. Neurobiology of aging 2015 Jan 36 (1): 546.e17-8. Lin Chin-Hsien, Lin Hang-I, Chen Meng-Ling, Wu Ruey-Me |
| Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy. Neurobiology of aging 2015 Feb 36 (2): 1222.e7-11. Chen Yong Ping, Zhao Bi, Cao Bei, Song Wei, Guo XiaoYan, Wei Qian-Qian, Yang Yuan, Yuan Li Xing, Shang Hui-Fa |
| Analysis of COQ2 gene in multiple system atrophy. Molecular neurodegeneration 2014 9 44. Ogaki Kotaro, Fujioka Shinsuke, Heckman Michael G, Rayaprolu Sruti, Soto-Ortolaza Alexandra I, Labbé Catherine, Walton Ronald L, Lorenzo-Betancor Oswaldo, Wang Xue, Asmann Yan, Rademakers Rosa, Graff-Radford Neill, Uitti Ryan, Cheshire William P, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
| Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis. PloS one 2015 10 (6): e0130970. Yang Xinglong, Xi Jing, Zhao Quanzhen, Jia Hua, An Ran, Liu Zhuolin, Xu Yanmi |
| Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy. CNS neuroscience & therapeutics 2015 Aug 21 (8): 626-30. Wen Xiao-Dan, Li Hong-Fu, Wang Hong-Xia, Ni Wang, Dong Yi, Wu Zhi-Yi |
| Association Analysis of COQ2 Variant in Dementia and Essential Tremor. Parkinson's disease 2015 2015 926280. Chao Yin Xia, Ng Ebonne Yu Lin, Li Huihua, Nagaendran Kandiah, Yih Yuen, Chong Mei Sian, Prakash Kumar M, Tan Louis, Au Wing Lok, Zhao Yi, Zhou Zhi Dong, Tio Murni, Pavanni Ratnagopal, Tan Eng Ki |
| Brain energy metabolism in early MSA-P: A phosphorus and proton magnetic resonance spectroscopy study. Parkinsonism & related disorders 2015 May 21 (5): 533-5. Stamelou M, Pilatus U, Reuss A, Respondek G, Knake S, Oertel W H, Höglinger G |
| [Susceptibility gene in multiple system atrophy (MSA)]. Rinsh? shinkeigaku = Clinical neurology 2014 54 (12): 969-71. Tsuji Sho |
| Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Nov . Zhao QuanZhen, Yang Xinglong, Tian SiJia, An Ran, Zheng JinHua, Xu Yanmi |
| Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Jul 36 (7): 1211-5. Yang Xinglong, Xi Jing, An Ran, Yu Lihua, Lin Zhenfang, Zhou Huayong, Xu Yanmi |
| COQ2 gene variants associate with cerebellar subtype of multiple system atrophy in Chinese. Movement disorders : official journal of the Movement Disorder Society 2015 Mar 30 (3): 436-7. Lin Chin-Hsien, Tan Eng-King, Yang Chih-Chao, Yi Zhao, Wu Ruey-Me |
| MAPT haplotype diversity in multiple system atrophy. Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
| Mutational analysis of COQ2 in patients with MSA in Italy. Neurobiology of aging 2016 Jun . Ronchi Dario, Di Biase Ernesto, Franco Giulia, Melzi Valentina, Del Sorbo Francesca, Elia Antonio, Barzaghi Chiara, Garavaglia Barbara, Bergamini Christian, Fato Romana, Mora Gabriele, Del Bo Roberto, Fortunato Francesco, Borellini Linda, Trezzi Ilaria, Compagnoni Giacomo Monzio, Monfrini Edoardo, Frattini Emanuele, Bonato Sara, Cogiamanian Filippo, Ardolino Gianluca, Priori Alberto, Bresolin Nereo, Corti Stefania, Comi Giacomo Pietro, Di Fonzo Aless |
| Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy. JAMA neurology 2016 Jun . Mitsui Jun, Matsukawa Takashi, Yasuda Tsutomu, Ishiura Hiroyuki, Tsuji Sho |
| New susceptible variant of COQ2 gene in Japanese patients with sporadic multiple system atrophy. Neurology. Genetics 2016 Apr 2 (2): e54. Sun Zhuoran, Ohta Yasuyuki, Yamashita Toru, Sato Kota, Takemoto Mami, Hishikawa Nozomi, Abe Ko |
A genome-wide association study in multiple system atrophy.
Neurology 2016 Sep . Sailer Anna, Scholz Sonja W, Nalls Michael A, Schulte Claudia, Federoff Monica, Price T Ryan, Lees Andrew, Ross Owen A, Dickson Dennis W, Mok Kin, Mencacci Niccolo E, Schottlaender Lucia, Chelban Viorica, Ling Helen, O'Sullivan Sean S, Wood Nicholas W, Traynor Bryan J, Ferrucci Luigi, Federoff Howard J, Mhyre Timothy R, Morris Huw R, Deuschl Günther, Quinn Niall, Widner Hakan, Albanese Alberto, Infante Jon, Bhatia Kailash P, Poewe Werner, Oertel Wolfgang, Höglinger Günter U, Wüllner Ullrich, Goldwurm Stefano, Pellecchia Maria Teresa, Ferreira Joaquim, Tolosa Eduardo, Bloem Bastiaan R, Rascol Olivier, Meissner Wassilios G, Hardy John A, Revesz Tamas, Holton Janice L, Gasser Thomas, Wenning Gregor K, Singleton Andrew B, Houlden Henry, |
| Serum Levels of Coenzyme Q10 in Patients with Multiple System Atrophy. PloS one 2016 11 (1): e0147574. Kasai Takashi, Tokuda Takahiko, Ohmichi Takuma, Ishii Ryotaro, Tatebe Harutsugu, Nakagawa Masanori, Mizuno Toshi |
| COQ2 variants in Parkinson's disease and multiple system atrophy. Journal of neural transmission (Vienna, Austria : 1996) 2018 4 125 (6): 937-944. Mikasa Michitaka, Kanai Kazuaki, Li Yuanzhe, Yoshino Hiroyo, Mogushi Kaoru, Hayashida Arisa, Ikeda Aya, Kawajiri Sumihiro, Okuma Yasuyuki, Kashihara Kenichi, Sato Tatsuya, Kondo Hiroshi, Funayama Manabu, Nishioka Kenya, Hattori Nobuta |
| Genetic mutation analysis of the COQ2 gene in Italian patients with multiple system atrophy. Gene 2019 Aug 144037. Procopio Radha, Gagliardi Monica, Brighina Laura, Nicoletti Giuseppe, Morelli Maurizio, Ferrarese Carlo, Annesi Grazia, Quattrone Al |
| Cerebral mitochondrial electron transport chain dysfunction in multiple system atrophy and Parkinson's disease. Scientific reports 2019 4 9 (1): 6559. Foti Sandrine C, Hargreaves Iain, Carrington Stephanie, Kiely Aoife P, Houlden Henry, Holton Janice |
| Reductions in COQ2 Expression Relate to Reduced ATP Levels in Multiple System Atrophy Brain. Frontiers in neuroscience 2019 13 1187. Hsiao Jen-Hsiang T, Purushothuman Sivaraman, Jensen Poul H, Halliday Glenda M, Kim Woojin Sco |
| COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian population. Journal of the neurological sciences 2021 8 429 117623. Porto Kristine Joyce, Hirano Makito, Mitsui Jun, Chikada Ayaka, Matsukawa Takashi, Ishiura Hiroyuki, , Toda Tatsushi, Kusunoki Susumu, Tsuji Sho |
| COQ2 and SNCA polymorphisms interact with environmental factors to modulate the risk of multiple system atrophy and subtype disposition. European journal of neurology 2022 Jun . Kuo Ming-Che, Lu Ying-Che, Tai Chun-Hwei, Soong Bing-Wen, Hu Fu-Chang, Chen Meng-Ling, Lin Chin-Hsien, Wu Ruey-Me |
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- Page last updated:Sep 25, 2023
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